Nayeri Hashem, Ali Naderi Gholam, Saleh Moghadam Masoud, Mohamadzadeh Samaneh, Boshtam Maryam, Jafari Dinani Narges, Abedpour Dehkordi Adel
Assistant Professor of Biochemistry, Islamic Azad University, Falavarjan Branch, Department of Biochemistry, Falavarjan, Iran.
ARYA Atheroscler. 2010 Fall;6(3):85-9.
Atherosclerosis is the most important underlying cause of cardiovascular diseases (CVD) which recently has been classified as an inflammatory disorder. Accumulation of large amounts of oxidized LDL in the intima during local inflammation reaction led to increase several factors such as C -reactive protein (CRP). It has also been reported that CRP is able to bind with modified forms of LDL as well as oxidized LDL. These findings suggest possible positive or negative involvement of this protein in atherogenesis. The main objective of the present study was to assess the influence of CRP on LDL oxidation and the possible physical \changes of LDL in the presence of CRP in vitro.
In this study, the susceptibility of purified LDL to oxidation was assayed by monitoring of formation of conjugated dienes in different physiological concentrations of CRP (0 - 0.5 -2 µg/ml) using a shimadzu spectrophotometer. Electrophoresis was used to determine the electrophoretic mobility of LDL in those conditions.
CRP significantly reduced the susceptibility of Cu(++) -induced LDL oxidation through increasing the lag timeand there was positive relationship between these findings and CRP concentration (P < 0.05). CRP caused a significant reduction in the electrophotretic mobility of LDL compared to native LDL (n-LDL) (P < 0.05).
A considerable reduction was shown in LDL oxidation, in higher concentration of CRP, via an unknown mechanism. The electrophoretic mobility of LDL, in the oxidative condition, decreases in the presence of CRP compared to n-LDL, which can be indicative of the effect of this protein on the physical and chemical properties of LDL. It seems that, other pathway than LDL oxidation is responsible for the effect of CRP on the atherogenesis processes.
动脉粥样硬化是心血管疾病(CVD)最重要的潜在病因,最近被归类为一种炎症性疾病。在局部炎症反应期间,大量氧化型低密度脂蛋白(LDL)在内膜中积聚导致多种因子增加,如C反应蛋白(CRP)。也有报道称,CRP能够与修饰形式的LDL以及氧化型LDL结合。这些发现表明该蛋白在动脉粥样硬化形成过程中可能具有正向或负向作用。本研究的主要目的是评估CRP对LDL氧化的影响以及在体外存在CRP时LDL可能发生的物理变化。
在本研究中,使用岛津分光光度计通过监测不同生理浓度的CRP(0 - 0.5 - 2μg/ml)中共轭二烯的形成来测定纯化LDL的氧化敏感性。采用电泳法测定在这些条件下LDL的电泳迁移率。
CRP通过延长滞后期显著降低了Cu(++)诱导的LDL氧化敏感性,这些结果与CRP浓度之间存在正相关(P < 0.05)。与天然LDL(n-LDL)相比,CRP导致LDL的电泳迁移率显著降低(P < 0.05)。
在较高浓度的CRP作用下,LDL氧化显著降低,其机制尚不清楚。与n-LDL相比,在氧化条件下,存在CRP时LDL的电泳迁移率降低,这可能表明该蛋白对LDL的物理和化学性质有影响。似乎CRP对动脉粥样硬化形成过程的影响是通过LDL氧化以外的其他途径实现的。